Haddock - 36987-1216-3 - (Haddock)

Alphabetical Index


Drug Information of Haddock

Product NDC: 36987-1216
Proprietary Name: Haddock
Non Proprietary Name: Haddock
Active Ingredient(s): .1    g/mL & nbsp;   Haddock
Administration Route(s): INTRADERMAL; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Haddock

Product NDC: 36987-1216
Labeler Name: Nelco Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA102192
Marketing Category: BLA
Start Marketing Date: 19720829

Package Information of Haddock

Package NDC: 36987-1216-3
Package Description: 30 mL in 1 VIAL, MULTI-DOSE (36987-1216-3)

NDC Information of Haddock

NDC Code 36987-1216-3
Proprietary Name Haddock
Package Description 30 mL in 1 VIAL, MULTI-DOSE (36987-1216-3)
Product NDC 36987-1216
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Haddock
Dosage Form Name INJECTION, SOLUTION
Route Name INTRADERMAL; SUBCUTANEOUS
Start Marketing Date 19720829
Marketing Category Name BLA
Labeler Name Nelco Laboratories, Inc.
Substance Name HADDOCK
Strength Number .1
Strength Unit g/mL
Pharmaceutical Classes Non-Standardized Food Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Allergens [Chemical/Ingredient],Dietary Proteins [Chemical/Ingredient],Fish Proteins, Dietary [Chemical/Ingredient]

Complete Information of Haddock


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